This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 33032, NP_000286.3:p.THR85MET

HGVS name

None

About this variant

This variant has 2504 sample genotypes and is associated with 4 phenotypes.

Variant displays